tyrosine and Albers-Schoenberg Disease

tyrosine has been researched along with Albers-Schoenberg Disease in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19902 (50.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ahariz, N; Cambisano, N; Charlier, C; Coppieters, W; Druet, T; Fasquelle, C; Jentsch, TJ; Ludwig, CF; Sartelet, A; Stauber, T; Zhang, Z1
Liu, J; Pei, D; Shu, X; Wang, Q; Xu, J; Xu, T; Ye, Y1
Groth, CG; Ringdén, O1
Francis, MJ; Macmillan, DC; Smith, R1

Reviews

1 review(s) available for tyrosine and Albers-Schoenberg Disease

ArticleYear
Transplantation in relation to the treatment of inherited disease.
    Transplantation, 1984, Volume: 38, Issue:4

    Topics: alpha 1-Antitrypsin Deficiency; Amyloidosis; Bone Marrow Transplantation; Fabry Disease; Gaucher Disease; Genetic Diseases, Inborn; Gout; Granulomatous Disease, Chronic; Hemoglobinopathies; Hemophilia A; Hepatolenticular Degeneration; Humans; Immunologic Deficiency Syndromes; Kidney Transplantation; Leukodystrophy, Metachromatic; Liver Transplantation; Lymphocytes; Metabolism, Inborn Errors; Mucopolysaccharidoses; Nephritis, Hereditary; Niemann-Pick Diseases; Osteopetrosis; Oxalates; Oxalic Acid; Transplantation; Tyrosine; Uremia

1984

Other Studies

3 other study(ies) available for tyrosine and Albers-Schoenberg Disease

ArticleYear
A missense mutation accelerating the gating of the lysosomal Cl-/H+-exchanger ClC-7/Ostm1 causes osteopetrosis with gingival hamartomas in cattle.
    Disease models & mechanisms, 2014, Volume: 7, Issue:1

    Topics: Amino Acid Sequence; Animals; Cattle; Chloride Channels; Genome-Wide Association Study; Genotype; Gingival Diseases; Hamartoma; Haplotypes; HeLa Cells; Homeostasis; Homozygote; Humans; Lysosomes; Membrane Proteins; Mice; Molecular Sequence Data; Mutation, Missense; Osteopetrosis; Sequence Homology, Amino Acid; Tyrosine; Ubiquitin-Protein Ligases; Xenopus laevis

2014
Structure of human SNX10 reveals insights into its role in human autosomal recessive osteopetrosis.
    Proteins, 2014, Volume: 82, Issue:12

    Topics: Amino Acid Sequence; Amino Acid Substitution; Arginine; Humans; MCF-7 Cells; Models, Molecular; Molecular Sequence Data; Mutation; Osteoclasts; Osteopetrosis; Protein Conformation; Protein Interaction Domains and Motifs; Protein Stability; Protein Structure, Tertiary; Protein Transport; Recombinant Proteins; Sequence Alignment; Sorting Nexins; Tyrosine; Vacuoles

2014
Polymeric collagen of skin in normal sunjects and in patients with inherited connective tissue disorders.
    Clinical science, 1973, Volume: 44, Issue:5

    Topics: Acromegaly; Adolescent; Adult; Aged; Child; Child, Preschool; Collagen; Collagen Diseases; Female; Hexosamines; Homocystinuria; Hot Temperature; Humans; Hyperparathyroidism; Male; Microscopy, Electron; Middle Aged; Myositis Ossificans; Osteitis Deformans; Osteogenesis Imperfecta; Osteopetrosis; Pseudoxanthoma Elasticum; Skin; Tyrosine; Werner Syndrome

1973